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The Journal of Biological Chemistry|April 29, 1994
Mutation of peptide binding site in transmembrane region of a G protein-coupled receptor accounts for endothelin receptor subtype selectivityS R Krystek, P S Patel, P M Rose, et al.The American Journal of Physiology|November 14, 1997
Hypoxia stimulates human preproendothelin-1 promoter activity in transgenic miceC R Aversa, S Oparil, J Caro, et al.Journal of Medicinal Chemistry|August 24, 2000
Biphenylsulfonamide endothelin receptor antagonists. 2. Discovery of 4'-oxazolyl biphenylsulfonamides as a new class of potent, highly selective ET(A) antagonistsN Murugesan, Z Gu, P D Stein, et al.Biochemistry|February 27, 1996
Mutational analysis of the endothelin type A receptor (ETA): interactions and model of selective ETA antagonist BMS-182874 with putative ETA receptor binding cavityM L Webb, P S Patel, P M Rose, et al.Immunopharmacology|December 22, 1999
Small molecule antagonists of the bradykinin B1 receptorR A Horlick, M H Ohlmeyer, I L Stroke, et al.Journal of Medicinal Chemistry|December 19, 1998
Biphenylsulfonamide endothelin antagonists: structure-activity relationships of a series of mono- and disubstituted analogues and pharmacology of the orally active endothelin antagonist 2'-amino-N- (3,4-dimethyl-5-isoxazolyl)-4'-(2-methylpropyl)[1, 1'-biphenyl]-2-sulfonamide (BMS-187308)N Murugesan, Z Gu, P D Stein, et al.Pageof 6